510(k) K830779 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PRESSURE FUNCTION BLOCK FOR BLOOD PRESS
| Applicant | Honeywell, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 9, 1983 |
| Received | Mar 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830779
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.